Human NAD(P)H:quinone oxidoreductase (NQO sub 1 ) gene structure and induction by dioxin
Journal Article
·
· Biochemistry; (United States)
- New York Univ. Medical Center, NY (United States) Fox Chase Cancer Center, Philadelphia, PA (United States)
The human NAD(P):quinone oxidoreductase (NQO{sub 1}) gene, 1850 base pairs (bp) of the 5{prime} flanking region, and 67 bp of the 3{prime} flanking region have been sequenced. The human NQO{sub 1} gene is approximately 20 kb in length and has six exons interrupted by five introns. The start site of transcription was determined by primer extension analysis. Nuclear run-on experiments performed using nuclei isolated from 2,3,7,8-tetrachlorodibenzo-p-doxin (TCDD) treated and untreated human hepatoblastoma (Hep-G2) cells demonstrated that TCDD treatment increases the rate of transcription of endogenous NQO{sub 1} gene by 3-fold. The sequence analysis of the 5{prime} flanking region of the NQO{sub 1} gene showed the presence of a TATA box in the {minus}37 to {minus}32 bp region, one CCAAT box at nucleotide {minus}649, an AP1 binding site at position {minus}462, an AP2 site at nucleotide position {minus}156, and one copy of the nucleotide sequence GCGTC. It is noteworthy that XRE in human NQO{sub 1} gene is located 5{prime} to the ARE compared to its 3{prime} location in the rat quinone reductase gene. Interestingly, the consensus sequence for binding to AP1 protein (TGACTCA) is contained within the ARE sequence (TCACAGTGACTCAGCAGAATC) of human NQO{sub 1} gene. By deletion mutagenesis and transfection studies, the author has identified a segment of DNA in the upstream region of the human NQO{sub 1} gene required for a high level of expression in hepatoma cells and its induction by TCDD.
- OSTI ID:
- 5687405
- Journal Information:
- Biochemistry; (United States), Journal Name: Biochemistry; (United States) Vol. 30:44; ISSN 0006-2960; ISSN BICHA
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
550201* -- Biochemistry-- Tracer Techniques
59 BASIC BIOLOGICAL SCIENCES
AMINO ACID SEQUENCE
ANIMALS
BETA DECAY RADIOISOTOPES
BETA-MINUS DECAY RADIOISOTOPES
BIOLOGICAL EFFECTS
DAYS LIVING RADIOISOTOPES
DIOXIN
DNA SEQUENCING
ENZYMES
GENES
HETEROCYCLIC COMPOUNDS
ISOTOPES
LIGHT NUCLEI
MAMMALS
MAN
MOLECULAR STRUCTURE
NUCLEI
ODD-ODD NUCLEI
ORGANIC COMPOUNDS
ORGANIC OXYGEN COMPOUNDS
OXIDOREDUCTASES
PHOSPHORUS 32
PHOSPHORUS ISOTOPES
PRIMATES
PROTEINS
RADIOISOTOPES
STRUCTURAL CHEMICAL ANALYSIS
VERTEBRATES
59 BASIC BIOLOGICAL SCIENCES
AMINO ACID SEQUENCE
ANIMALS
BETA DECAY RADIOISOTOPES
BETA-MINUS DECAY RADIOISOTOPES
BIOLOGICAL EFFECTS
DAYS LIVING RADIOISOTOPES
DIOXIN
DNA SEQUENCING
ENZYMES
GENES
HETEROCYCLIC COMPOUNDS
ISOTOPES
LIGHT NUCLEI
MAMMALS
MAN
MOLECULAR STRUCTURE
NUCLEI
ODD-ODD NUCLEI
ORGANIC COMPOUNDS
ORGANIC OXYGEN COMPOUNDS
OXIDOREDUCTASES
PHOSPHORUS 32
PHOSPHORUS ISOTOPES
PRIMATES
PROTEINS
RADIOISOTOPES
STRUCTURAL CHEMICAL ANALYSIS
VERTEBRATES